Page last updated: 2024-08-01 21:24:06

icariside i

Description

icariside I: structure in first source [MeSH]

Cross-References

ID SourceID
PubMed CID5745470
CHEMBL ID558499
SCHEMBL ID4215872
MeSH IDM0518891

Synonyms (27)

Synonym
baohuoside-1
3,5,7-trihydroxy-4'-methoxy-8'-prenylflavone-3-o-alpha-l-rhamnopranoxide
4h-1-benzopyran-4-one, 3,5-dihydroxy-7-(beta-d-glucopyranosyloxy)-2-(4-methoxyphenyl)-8-(3-methyl-2-butenyl)-
brn 0072036
icariside i
CHEMBL558499
3,5-dihydroxy-2-(4-methoxyphenyl)-8-(3-methylbut-2-enyl)-7-[(2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one
56725-99-6
4-18-00-03374 (beilstein handbook reference)
S3247
AKOS016013487
SCHEMBL4215872
lcariside i
AC-34999
icariside-i
icarisid i
DTXSID30205283
CS-0018250
3,5-dihydroxy-2-(4-methoxyphenyl)-8-(3-methylbut-2-en-1-yl)-7-(((2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2h-pyran-2-yl)oxy)-4h-chromen-4-one
HY-N1939
mfcd01662755
3,5-dihydroxy-2-(4-methoxyphenyl)-8-(3-methyl-2-buten-1-yl)-4-oxo-4h-chromen-7-yl beta-d-glucopyranoside
IYCPMVXIUPYNHI-WPKKLUCLSA-N
icariside 1
icariin i
AS-78068
icarisidei

Bioassays (1)

Assay IDTitleYearJournalArticle
AID428313Reversal of P-gp-mediated multidrug resistance in human MCF7 cells assessed as assessed as increase in intracellular adriamycin accumulation at 5 uM incubated 2 hrs before adriamycin challenge by spectrophotometry2009Bioorganic & medicinal chemistry letters, Aug-01, Volume: 19, Issue:15
ISSN: 1464-3405
Synthesis and antimultidrug resistance evaluation of icariin and its derivatives.

Research

Studies (7)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's3 (42.86)29.6817
2010's0 (0.00)24.3611
2020's4 (57.14)2.80

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other7 (100.00%)84.16%
SubstanceStudiesClassesRolesFirst YearLast YearAverage AgeRelationship StrengthTrialspre-19901990's2000's2010'spost-2020
ketoconazoledichlorobenzene;
dioxolane;
ether;
imidazoles;
N-acylpiperazine;
N-arylpiperazine
2009200915.0low000100
icaritin2009200915.0low000100
icariinflavonols;
glycosyloxyflavone
antioxidant;
bone density conservation agent;
EC 3.1.4.35 (3',5'-cyclic-GMP phosphodiesterase) inhibitor;
phytoestrogen
2009200915.0low000100
baohuoside iglycosyloxyflavoneanti-inflammatory agent;
antineoplastic agent;
apoptosis inducer;
plant metabolite
2009200915.0low000100
SubstanceStudiesClassesRolesFirst YearLast YearAverage AgeRelationship StrengthTrialspre-19901990's2000's2010'spost-2020
indoleindole;
polycyclic heteroarene
Escherichia coli metabolite202120213.0low000001
kynureninearomatic ketone;
non-proteinogenic alpha-amino acid;
substituted aniline
human metabolite202220222.0low000001
nigericinpolycyclic etherantibacterial agent;
antimicrobial agent;
bacterial metabolite;
potassium ionophore
202120213.0low000001
daidzein7-hydroxyisoflavonesantineoplastic agent;
EC 2.7.7.7 (DNA-directed DNA polymerase) inhibitor;
EC 3.2.1.20 (alpha-glucosidase) inhibitor;
phytoestrogen;
plant metabolite
2007200717.0low000100
icaritin2008200816.0low000100
icariinflavonols;
glycosyloxyflavone
antioxidant;
bone density conservation agent;
EC 3.1.4.35 (3',5'-cyclic-GMP phosphodiesterase) inhibitor;
phytoestrogen
2007200816.5medium000200
baohuoside iglycosyloxyflavoneanti-inflammatory agent;
antineoplastic agent;
apoptosis inducer;
plant metabolite
2007202211.7high000201
ConditionIndicatedStudiesFirst YearLast YearAverage AgeRelationship StrengthTrialspre-19901990's2000's2010'spost-2020
Acute Liver Injury, Drug-Induced0202120213.0medium000001
Benign Neoplasms0202220222.0medium000001
Chemical and Drug Induced Liver Injury0202120213.0medium000001
Disease Models, Animal0202120213.0medium000001
Malignant Melanoma0202120213.0medium000001
Melanoma0202120213.0medium000001
Neoplasms0202220222.0medium000001
Sensitivity and Specificity02007200717.0medium000100

Safety/Toxicity (1)

ArticleYear
Icariside I specifically facilitates ATP or nigericin-induced NLRP3 inflammasome activation and causes idiosyncratic hepatotoxicity.
Cell communication and signaling : CCS, , 02-11, Volume: 19, Issue:1
2021